Canonical Allele Identifier: CA14690118
Gene: XRCC1 HGNC NCBI

Linked Data

dbSNP Id: rs3213368
gnomAD v2: 19-44055644-G-A
gnomAD v3: 19-43551492-G-A
gnomAD v4: 19-43551492-G-A
MyVariant Identifiers: chr19:g.44055644G>A (hg19) chr19:g.43551492G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.43551492G>A , CM000681.2:g.43551492G>A GRCh38
NC_000019.9:g.44055644G>A , CM000681.1:g.44055644G>A GRCh37
NC_000019.8:g.48747484G>A NCBI36
NG_033799.1:g.29087C>T , LRG_784:g.29087C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000262887.10:c.1199+79C>T MANE Select ENSP00000262887.5:n.1199+79C>T
ENST00000262887.9:c.1199+79C>T ENSP00000262887.4:n.1199+79C>T
ENST00000543982.5:c.1106+79C>T ENSP00000443671.1:n.1106+79C>T
NM_006297.2:c.1199+79C>T , LRG_784t1:c.1199+79C>T NP_006288.2:n.1199+79C>T
NM_006297.3:c.1199+79C>T MANE Select NP_006288.2:n.1199+79C>T
Search 100 bp 5'
Search 100 bp 3'